Moira Cheung

Consultant in Paediatric Endocrinology and Rare Bone Conditions. @GOSH @ELCH. SDG and SDMC committees. holistic, family centred care, robust science, teaching

[Prof Amaka C Offiah @ACOffiah]

@ADC_BMJ @GOSH_NeuroSurg Great work led by @moiracheung concluding that all infants with achondroplasia AFMS3 should have MRI at 6m of age.

[ADC @ADC_BMJ]

Natural history of spinal cord compression stage AFMS3 in infants with achondroplasia

40% progress and undergo neurosurgery
Suggest all have MRI at 6m

Retrospective cohort study 🇬🇧
@ACOffiah @GOSH_NeuroSurg
https://t.co/DA9HuBmYcP

[Moira Cheung @moiracheung]

@UkXlh Congratulations! This is wonderful news for all our patients! Well done on such a strong patient advocacy group. It makes ALL the difference

[ISCBH @childrensbones]

Just 4 days to go until #ICCBH2024 and it's not too late to register!

[ISCBH @childrensbones]

There are still a few places left on the ISCBH/@ern_bond Achondroplasia workshop at #ICCBH2024 so register soon!
https://t.co/BiL2qHBlmh

[Moira Cheung @moiracheung]

Only 4 replies from uk so far! Come on uk!

[Moira Cheung @moiracheung]

This will be shared with top international doctors involved in the care on Achon.. please help to more fully inform them

[Moira Cheung @moiracheung]

We would love to hear your voice on this! This is going internationally but would especially love UK representation in the results.

[Moira Cheung @moiracheung]

@GreatOrmondSt I remember sister Lindy from my Sho gosh days on parrot.. over 20 years ago… she was someone who showed me what great leadership looked like. Congratulations! Wonderful News!

[Moira Cheung @moiracheung]

@ACHONforum Thank you for beautiful lectures. It’s important that if there is Obstructive SA not to delay screening for Foramen magnum stenosis as a cause. It’s also why we don’t use sedation for the MRI and it can lead to an unsafe airway.

[Moira Cheung @moiracheung]

SDMC working hard 2023

[Moira Cheung @moiracheung]

SDMC Denver

[Brittle Bone Society @BrittleBoneUK]

The BBS & friends in the Rare Bone Alliance celebrated the launch of the NHS Rare Disease Collaborative Network for Adult Rare Bone. It was a successful day of networking and informative talks with reps from the 19 NHS Hospitals who have joined! Read more: https://t.co/aDnNA8If8J

[Oliver Gardiner @otronics]

@UkXlh @DMAILhealth @EnnalsEthan @rebecwhitt Pleading for help here! @GeneticAll_UK @rarediseaseuk

[Klane K White MD @KlaneKWhiteMD]

What a fantastic meeting! Making friends across the pond. 🇺🇸🇬🇧
Autumn UK Skeletal Dysplasia Meeting: “Stick or Twist”
Larsen Syndrome, Multiple Synostoses Syndromes and so much more!

[Endocrine Connections @EndoConnect]

👏Congratulations to @LChan_3 @QMUL, one of our Senior Editors on winning the @Soc_Endo Starling Medal for contributing to exceptional scientific advances in #endocrinology. At #SfeBES2023 Dr Chan explores Melanocortin Receptors & their accessory proteins in health & disease.

[Jarod Wong @drjarodwong]

Delighted with this research award for our study “Collaborative devt of national education standards & resources for emerg. mgt of adrenal insufficiency: mixed-model multiphase study” led by @LucyBray9 #BSPED2023 @mayng888 @AddisonsUK @Pituitary_org @BritSPED

[Moira Cheung @moiracheung]

@JudeBubbear Amazing Jude. Hope you enjoyed it ❤️